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T10644c-Fms-IN-10；化合物 T10644c-Fms-IN-10
c-Fms-IN-10 is the derivative of thieno [3,2-d] pyrimidine, a kinase inhibitor of FMS (Colony-stimulating factor-1 receptor, CSF-1R; IC50: 2 nM) with anti-tumor activity.
价 格：￥电议型 号：T10644产 地：中国大陆
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T10643c-Fms-IN-1；化合物c-Fms-IN-1c-Fms-IN-1
c-Fms-IN-1 is an inhibitor of c-FMS kinase (IC50 = 0.8 nM).
价 格：￥电议型 号：T10643产 地：中国大陆
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T10642c-di-AMP；环二腺苷酸Cyclic diadenylate|||Cyclic-di-AMP；环二腺苷酸|||Cyclic diadenylate|||Cyclic-di-AMP
c-di-AMP (Cyclic diadenylate) is a STING agonist. It binds to the transmembrane protein STING thereby activating the TBK3-IRF3 signaling pathway.
价 格：￥电议型 号：T10642产 地：中国大陆
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T10641C-82；化合物C-82C-82
C-82 is a specific CBP/β-catenin antagonist. It inhibits the binding between β-catenin and CBP and increases the binding between β-catenin and p300.
价 格：￥电议型 号：T10641产 地：中国大陆
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T10640C-11；化合物 T10640C-11
C-11 is a tubulin inhibitor and acts as an ADC cytotoxin with cytotoxicity for carcinoma cell lines.
价 格：￥电议型 号：T10640产 地：中国大陆
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T1064Norepinephrine bitartrate monohydrate；酒石酸去甲肾上腺素Levophed|||Noradrenaline bitartrate monohydrate；酒石酸去甲
Norepinephrine bitartrate monohydrate (Levophed) is a direct alpha-adrenergic receptors stimulator.
价 格：￥电议型 号：T1064产 地：中国大陆
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T10608BRD5648；化合物BRD5648(R)-BRD0705；(R)-BRD0705
BRD5648 ((R)-BRD0705) is an inactive (R)-enantiomer of BRD0705. BRD0705 is a GSK3α inhibitor (IC50: 66 nM; Kd: 4.8 μM) and can be used in acute myeloid leukemia (AML) studies.
价 格：￥电议型 号：T10608产 地：中国大陆
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T10605BRD-K98645985；化合物 T10605BRD-K98645985
BRD-K98645985 is a BAF transcriptional repression inhibitor (EC50: ~2.37 μM). It binds ARID1A-specific BAF complexes, potently reverses HIV-1 latency and prevents nucleosomal positioning.
价 格：￥电议型 号：T10605产 地：中国大陆
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T10564(8R,9S)-Talazoparib；他拉唑帕利 (8R,9S)(8R,9S)-BMN-673；(8R,9S)-BMN-673|||他拉唑帕利 (8R,9S)
(8R,9S)-Talazoparib is Talazoparib enantiomer , less active than Talazoparib on the inhibition of PARP1 (IC50: 144 nM).
价 格：￥电议型 号：T10564产 地：中国大陆
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T10531BGB-102；化合物 BGB-102JNJ-26483327；JNJ-26483327
BGB-102 (JNJ-26483327) is a kinase inhibitor targeting FLT3 and YES1 and an antagonist targeting EGFR and VEGFR3, which may be useful in the study of macular degeneration and diseases associated with genetic disorders and malformations.
价 格：￥电议型 号：T10531产 地：中国大陆
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T10495LBefiradol化合物 T10495LNLX-112|||F13640
Befiradol (NLX-112) is an agonist of 5-HT1A receptor.
价 格：￥电议型 号：T10495L产 地：中国大陆
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T10468Elimusertib hydrochloride(1876467-74-1 free base)；化合物 Elimusertib hydrochlorideBAY-1895344 hydrochlo
Elimusertib hydrochloride(1876467-74-1 free base) (BAY-1895344 hydrochloride) is a effective, orally available and selective ATR inhibitor with anti-tumor activity.
价 格：￥电议型 号：T10468产 地：中国大陆
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T10464LAtuveciclib Racemate；阿维西利BAY-1143572 Racemate；BAY-1143572 Racemate|||阿维西利
Atuveciclib Racemate (BAY-1143572 Racemate) is the racemate mixture of Atuveciclib, which is a potent and highly selective, oral P-TEFb/CDK9 inhibitor which supresses CDK9/CycT1 with an IC50 of 13 nM.
价 格：￥电议型 号：T10464L产 地：中国大陆
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T10464Atuveciclib；化合物 T10464BAY-1143572；BAY-1143572
Atuveciclib (BAY-1143572) is a potent and highly selective, oral PTEFb / CDK9 inhibitor that inhibits CDK9 / CycT1 with an IC 50 of 13 nM [1].
价 格：￥电议型 号：T10464产 地：中国大陆
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T10429Tizaterkib；化合物AZD-0364AZD-0364；AZD-0364
Tizaterkib (AZD-0364) is a potent and selective ERK2 inhibitor.
价 格：￥电议型 号：T10429产 地：中国大陆
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T10364Arbutamine；阿布他明GP 21213；GP 21213
Arbutamine (GP 21213) is a novel potent non-selective beta-adrenoceptor agonist with alpha-1-sympathomimetic activity.Arbutamine promotes cardiac stress and increases heart rate, cardiac contractility.Arbutamine can be used to study cardiac stress and coronary artery disease
价 格：￥电议型 号：T10364产 地：中国大陆
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T10319LAnamorelin Fumarate；富马酸阿拉莫林ONO-7643 Fumarate|||RC1291 Fumarate；ONO-7643 Fumarate|||RC1291 Fumarate||
Anamorelin Fumarate is a novel ghrelin receptor agonist (EC50: 0.74 nM in the FLIPR assay).
价 格：￥电议型 号：T10319L产 地：中国大陆
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T10298L2AMG-548 dihydrochloride (864249-60-5 free base)；化合物 T10298L2AMG-548 dihydrochloride；AMG-548 dihydroc
AMG-548 dihydrochloride is an orally active and selective p38α inhibitor (Ki: 0.5 nM) and shows slightly selective over p38β (Ki: 36 nM) and >1000 fold selective against p38γ/p38δ. It is also extremely potent in the inhibition of whole blood LPS stimulated TNFα (IC50: 3 nM).
价 格：￥电议型 号：T10298L2产 地：中国大陆
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T10298AMG-548 hydrochloride (864249-60-5 free base)；化合物 T10298AMG-548 hydrochloride；AMG-548 hydrochloride
AMG-548 hydrochloride is an orally active and selective p38α inhibitor (Ki: 0.5 nM) and shows slightly selective over p38β (Ki: 36 nM) and >1000 fold selective against p38γ/p38δ. It is also extremely potent in the inhibition of whole blood LPS stimulated TNFα (IC50: 3 nM).
价 格：￥电议型 号：T10298产 地：中国大陆
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T10292AM-6494；化合物 T10292AM-6494
AM-6494 is a potent and orally active BACE1 inhibitor (IC50: 0.4 nM) with in vivo selectivity over BACE2 (IC50: 18.6 nM).
价 格：￥电议型 号：T10292产 地：中国大陆
